HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 717106Generated: October 31, 2026
Potassium Acetate → HCID 89812885, compound
https://huagongshe.com/reaction/717106
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | Bis(pinacolato)diborane | HCID 2733548 | — |
| Reactant | HCID 89812826 | HCID 89812826 | — |
| Catalyst | Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+) | HCID 178418228 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 89812885 | HCID 89812885 | 71.4% |
Reaction Steps
(5-Bromo-pyrimidin-2-yl)-(4-cyclopropylmethyl-piperazin-1-yl)-methanone (46 mg, 0.14 mmol), bis(pinacolato)diboron (43 mg, 0.17 mmol), Pd(dppf)Cl2 (12 mg, 0.014 mmol) and potassium acetate (42 mg, 0.42 mmol) in 1,4-dioxane (0.7 mL) were added to a microwave vial and the reaction mixture purged with N2 for 10 min. The reaction mixture was irradiated using a microwave reactor (300 W, 120° C., 20 min). The reaction mixture was passed through a Si-thiol cartridge (2 g) and the column washed with MeOH (4× column volumes). The solvent was removed in vacuo and purified by reverse phase preparative HPLC-MS. The sample was passed through a SCX-2 cartridge (500 mg) and the column washed with MeOH (4× column volumes). The compound was eluted from the column with 0.5M NH3/MeOH to afford 2-(4-cyclopropylmethyl-piperazine-1-carbonyl)-pyrimidine-5-boronic acid as a white solid (29 mg, 70%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09193689B2 |
|---|
| Source dataset | uspto-grants-2015_11 |
|---|
| ORD ID | ord-c5b03f48a4ac46d59138d44ef64f354e |
|---|
| Source note | uspto-grants-2015_11 |
|---|